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Structure of 99368-67-9
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2-Chloro-5-nitro-3-(trifluoromethyl)pyridine features a trifluoromethyl group flanked by electron-withdrawing chlorine and nitro substituents, creating a highly electrophilic pyridine core. This combination enables efficient coupling reactions in pharmaceutical synthesis, particularly in constructing complex heterocyclic scaffolds under mild conditions. The molecule exhibits excellent stability during handling and storage.
2-Chloro-5-nitro-3-(trifluoromethyl)pyridine serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its reactive chloropyridine moiety. The trifluoromethyl and nitro groups confer enhanced electron-withdrawing character, facilitating nucleophilic substitution and enabling access to substituted pyridine scaffolds relevant to agrochemical and pharmaceutical development. Its bench-stable crystalline form simplifies handling and purification in multi-step syntheses.
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GHS Pictogram :
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GHS No : GHS05,GHS06
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Signal Word : Danger
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UN#: 2810
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H315-H318-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: